U.S. patent number 8,118,782 [Application Number 12/875,713] was granted by the patent office on 2012-02-21 for insulin pump with replacement capabilities.
This patent grant is currently assigned to Roche Diagnostics International AG. Invention is credited to Axel Remde.
United States Patent |
8,118,782 |
Remde |
February 21, 2012 |
**Please see images for:
( Certificate of Correction ) ** |
Insulin pump with replacement capabilities
Abstract
Insulin delivery systems include a first insulin pump and a
second insulin pump, wherein each pump includes a memory configured
to store an infusion program, a control unit configured to control
operation of the pump, and a communication interface for data
exchange with the other pump, wherein the control unit of the first
insulin pump is configured monitor, a status of the first insulin
pump, activate a search for the presence of the second insulin pump
when a predetermined status is assumed, and, upon detection of the
presence of the second insulin pump, transmit, via the
communication interface of the first insulin pump, the infusion
program stored, and the control unit of the second insulin pump is
configured to search for the presence of the first insulin pump,
and, upon detection of the presence of the first insulin pump,
receive and store, the infusion program.
Inventors: |
Remde; Axel (Luetzelfueh,
CH) |
Assignee: |
Roche Diagnostics International
AG (Steinhausen, CH)
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Family
ID: |
39720385 |
Appl.
No.: |
12/875,713 |
Filed: |
September 3, 2010 |
Prior Publication Data
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Document
Identifier |
Publication Date |
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US 20110218495 A1 |
Sep 8, 2011 |
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Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
Issue Date |
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PCT/EP2009/001458 |
Mar 2, 2009 |
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Foreign Application Priority Data
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Mar 3, 2008 [EP] |
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08405064 |
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Current U.S.
Class: |
604/151; 607/60;
709/237; 709/232; 705/2 |
Current CPC
Class: |
G16H
40/67 (20180101); A61M 5/14248 (20130101); G16H
20/17 (20180101); G16H 40/40 (20180101); A61M
2205/6018 (20130101); A61M 2205/3569 (20130101); A61M
2205/3592 (20130101) |
Current International
Class: |
A61M
5/142 (20060101) |
Field of
Search: |
;604/151 ;607/2,60
;709/232,237,248 ;705/2 |
References Cited
[Referenced By]
U.S. Patent Documents
Foreign Patent Documents
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0010628 |
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Mar 2000 |
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WO |
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2006097453 |
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Sep 2006 |
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WO |
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2007056592 |
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May 2007 |
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WO |
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Other References
International Search Report, completion date of Aug. 5, 2009 for
International Application No. EP 09001458, pp. 1-8. cited by other
.
Written Opinion, mailing date of Nov. 8, 2009 for International
Application No. EP 09001458, pp. 1-8. cited by other.
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Primary Examiner: Vu; Quynh-Nhu H
Attorney, Agent or Firm: Dinsmore & Shohl LLP
Parent Case Text
CROSS REFERENCE TO RELATED APPLICATIONS
This application is a continuation of International Application No.
PCT/EP2009/001458 filed Mar. 2, 2009 which claims priority to
European Patent Application No. EP 08 405 064.0 filed on Mar. 3,
2008, both of which are incorporated by reference herein.
Claims
The invention claimed is:
1. An insulin delivery system comprising a first insulin pump and a
second insulin pump, wherein each of the first insulin pump and the
second insulin pump comprises: a memory configured to store an
infusion program; a control unit configured to control operation of
the insulin pump; and a communication interface for data exchange
with the other of the first insulin pump and the second insulin
pump; wherein the control unit of the first insulin pump is
configured to autonomously: monitor, during operation of the first
insulin pump according to the infusion program, a status of the
first insulin pump; activate a search for the presence of the
second insulin pump when a predetermined status is assumed by the
first insulin pump, wherein the control unit is further configured
to control the first insulin pump to continue insulin delivery
according to the infusion program during the search for the
presence of the second insulin pump is active; and, upon detection
of the presence of the second insulin pump, transmit, via the
communication interface of the first insulin pump, the infusion
program stored in the memory of the first insulin pump to the
second insulin pump; and the control unit of the second insulin
pump is configured to: search for the presence of the first insulin
pump, and, upon detection of the presence of the first insulin
pump, receive, via the communication interface of the second
insulin pump, an infusion program from the first insulin pump; and
store the infusion program in the memory of the second insulin
pump.
2. The insulin delivery system of claim 1, wherein the first
insulin pump and the second insulin pump are identical insulin
pumps.
3. A method for replacing a first insulin pump by a second insulin
pump, the method comprising: operating the first insulin pump
according to an infusion program stored in a memory of the first
insulin pump; and controlling the first insulin pump to
autonomously perform the steps of: activating a search for the
presence of the second insulin pump, wherein the first insulin pump
continues to operate to delivery insulin according to the infusion
program during the search for the presence of the second insulin
pump is active, and, upon detection of the presence of the second
insulin pump; and transmitting, via communication interfaces of the
first insulin pump and the second insulin pump, the infusion
program from the first insulin pump to the second insulin pump.
4. An insulin pump comprising: a communication interface for data
exchange with a replacement pump; a memory configured to store an
infusion program; and a control unit configured to control
operation of the insulin pump, wherein the control unit is further
configured to autonomously: monitor, during operation of the
infusion pump according to the infusion program, a status of the
insulin pump; activate a search for the presence of the replacement
pump when a predetermined status is assumed by the insulin pump,
wherein the control unit is further configured to control the
insulin pump to continue insulin delivery according to the infusion
program during the search for the presence of the replacement pump
is active; and transmit, upon detecting the presence of the
replacement pump, via the communication interface, the infusion
program stored in the memory to the replacement pump.
5. The insulin pump of claim 4, wherein the status monitored by the
control unit comprises at least one of a filling state of an
insulin reservoir of the insulin pump, the status of a battery of
the insulin pump, and an error status of the insulin pump.
6. The insulin pump of claim 5, wherein the control unit is further
configured to control the insulin pump to continue insulin delivery
while a search for the presence of the replacement pump is
active.
7. The insulin pump of claim 6, wherein the control unit is further
configured to control the insulin pump to terminate operation after
successful transmission of the infusion program to the replacement
pump.
8. The insulin pump of claim 7, wherein the insulin pump comprises,
in addition to the wireless communication interface, a device for
detecting the presence of the replacement pump.
9. The insulin pump of claim 8, wherein the insulin pump is further
configured to receive the infusion program from a remote
controller.
10. The insulin pump of claim 9, wherein the control unit is
further configured to indicate, via an indicator of the insulin
pump, at least one of the search for the replacement pump, the
successful detection of the replacement pump, the successful
transmission of the program to the replacement pump, or the
unsuccessful transmission of the program to the replacement
pump.
11. The insulin pump of claim 4, wherein the control unit is
further configured to control the insulin pump to terminate
operation after successful transmission of the infusion program to
the replacement pump.
12. The insulin pump of claim 4, wherein the insulin pump
comprises, in addition to the wireless communication interface, a
device for detecting the presence of the replacement pump.
13. The insulin pump of claim 4, wherein the insulin pump is
further configured to receive the infusion program from a remote
controller.
14. The insulin pump of claim 4, wherein the control unit is
further configured to indicate, via an indicator of the insulin
pump, at least one of the search for the replacement pump, the
successful detection of the replacement pump, the successful
transmission of the program to the replacement pump, or the
unsuccessful transmission of the program to the replacement
pump.
15. The insulin pump of claim 4, wherein the insulin pump is
further configured to: search for the presence of a source pump;
and when the presence of a source pump is detected, receive, via
the communication interface, an infusion program from the source
pump; and store the infusion program in the memory.
16. The insulin pump of claim 15, wherein the control unit is
further configured to detect an insulin reservoir of the insulin
pump being filled, and, upon the insulin reservoir being filled, to
activate the search for a source pump.
17. The insulin pump of claim 15, wherein the control unit is
further configured to control the insulin pump, after successfully
having received an infusion program from the source pump, to
autonomously start insulin delivery.
18. The insulin pump of claim 17, wherein the control unit is
further configured to detect an insulin reservoir of the insulin
pump being filled, and, upon the insulin reservoir being filled, to
activate the search for a source pump.
Description
TECHNICAL FIELD
The invention relates to insulin delivery systems and, more
specifically, insulin delivery systems including a first insulin
pump and a second insulin pump allowing for the replacement of the
first insulin pump by the second insulin pump via autonomous
program transfer.
BACKGROUND
Remotely controlled insulin pumps may be used for the continuous
subcutaneous infusion of insulin to patients with diabetes. The
insulin, which may be present in a reservoir of the insulin pump,
can be conveyed into the patient's body according to a patient and
time-of-day dependent basal delivery schedule via a subcutaneous
cannula. In addition to this basal delivery, bolus insulin delivery
may be performed out of the same reservoir on demand such as, for
example, for compensating carbohydrate intake and for correcting
undesirably raised blood glucose values. Some modern insulin pumps
have programmable remote controllers that can comprise a design
similar to a cell phone or a PDA. Alternatively, a standard device
such as a cell phone or a PDA may be used as the remote controller
itself. For those insulin pumps, the user interface of the insulin
pump itself may be limited or missing.
Insulin pumps which are designed to be fully remote controlled may
be disposable pumps which are designed to be used for a number of
days and to be disposed afterwards. When such a pump is replaced,
an infusion program including all required control data, such as
the basal delivery schedule, the date and the time of day may be
transferred onto the new pump from the remote controller. Prior to
this transfer, the memory of the insulin pump comprises the control
firmware but no patient-specific infusion program.
Some insulin pumps can be designed as patch pumps which are carried
by the patient directly at the infusion site and can be fixed to
the skin by an adhesive layer. Those pumps can comprise a cannula
and an automatic inserter which automatically inserts the cannula
into to patient's subcutaneous tissue from an initially retracted
position inside the housing. Those pumps may also be provided with
a readily built-in reservoir which is filled by the patient prior
to use and readily built-in battery. After a using time of some
days, the pump can be disposed as a whole.
For fully remote controlled insulin pumps, the remote controller
may be required for all user operations such as programming the
delivery of an insulin bolus or replacing the pump by a new one.
However, in some situations a remote controller may not be
available. This may be the case, for example, when the remote
controller is defective, lost or forgotten, e.g., when traveling.
Accordingly, a need exists for alternative insulin delivery systems
such as those including a first insulin pump and a second insulin
pump for continuous therapy.
SUMMARY
In one embodiment, an insulin delivery system includes a first
insulin pump and a second insulin pump. Each of the first insulin
pump and the second insulin pump includes a memory configured to
store an infusion program, a control unit configured to control
operation of the insulin pump, and a communication interface for
data exchange with the other of the first insulin pump and the
second insulin pump. The control unit of the first insulin pump is
configured to autonomously perform the steps of monitoring, during
operation of the first insulin pump according to the infusion
program, a status of the first insulin pump, activating a search
for the presence of the second insulin pump when a predetermined
status is assumed by the first insulin pump, and, upon detection of
the presence of the second insulin pump, transmitting, via the
communication interface of the first insulin pump, the infusion
program stored in the memory of the first insulin pump to the
second insulin pump. The control unit of the second insulin pump is
configured to perform the steps of searching for the presence of
the first insulin pump, and, upon detection of the presence of the
first insulin pump, performing the steps of receiving, via the
communication interface of the second insulin pump, an infusion
program from the first insulin pump and storing the infusion
program in the memory of the second insulin pump.
In another embodiment, a method for replacing a first insulin pump
by a second insulin pump, includes operating the first insulin pump
according to an infusion program stored in a memory of the first
insulin pump, and controlling the first insulin pump to
autonomously perform the steps of activating a search for the
presence of the second insulin pump, and, upon detection of the
presence of the second insulin pump, and transmitting, via
communication interfaces of the first insulin pump and the second
insulin pump, the infusion program from the first insulin pump to
the second insulin pump.
In yet another embodiment An insulin pump includes a communication
interface for data exchange with a replacement pump, a memory which
can be configured to store an infusion program, and a control unit
which is configured to control operation of the insulin pump. The
control unit can be configured to autonomously perform the steps of
monitoring, during operation of the infusion pump according to the
infusion program, a status of the insulin pump, activating a search
for the presence of the replacement pump when a predetermined
status is assumed by the insulin pump, and transmitting, upon
detecting the presence of the replacement pump, via the
communication interface, the infusion program stored in the memory
to the replacement pump.
BRIEF DESCRIPTION OF THE DRAWINGS
The embodiments set forth in the drawings are illustrative and
exemplary in nature and not intended to limit the subject matter
defined by the claims. The following detailed description of the
illustrative embodiments can be understood when read in conjunction
with the following drawings where like structure is indicated with
like reference numerals and in which:
FIG. 1 schematically depicts a replacement procedure of a first
insulin pump by a second insulin pump according to one or more
embodiments shown and described herein;
FIG. 2 depicts a plan view of the rear face of an insulin pump
according to one or more embodiments shown and described
herein;
FIG. 3 depicts a side view of the insulin pump from FIG. 2
according to one or more embodiments shown and described
herein;
FIG. 4 depicts a schematic view of the inner area and the
functional elements of the insulin pump in a cross section along
the line A-B in FIG. 2 according to one or more embodiments shown
and described herein;
FIG. 5 depicts a schematic sequence of deactivation of a source
pump which is in delivery mode, with the insulin reservoir almost
used up, and which is exchanged for a new replacement pump
according to one or more embodiments shown and described herein;
and
FIG. 6 depicts a schematic sequence of the steps involved in the
activation of the new replacement pump according to one or more
embodiments shown and described herein.
DETAILED DESCRIPTION
Insulin pumps and insulin delivery systems as disclosed herein may
allow a diabetic patient to continue their insulin pump therapy if
a first insulin pump has to be replaced. The insulin pumps may be
of any general type of insulin pump. For example, in one
embodiment, disposable patch pumps may be used. However, various
other insulin pumps may additionally or alternatively be
implemented as will become appreciated herein.
Referring now to FIGS. 1-6, in one embodiment, an insulin delivery
system may generally comprise a first insulin pump 1, 505 (also
referred to as a source pump) and a second insulin pump 1, 505'
(also referred to as a replacement pump). Referring specifically to
FIGS. 2-4, the first insulin pump 1 and the second insulin pump 1
may generally comprise a housing 2 in the form of a hollow
parallelepipedal body with rounded corners and edges or any other
form operable to house the necessary components as should become
appreciated herein. In other embodiments, the shape of the housing
2 may comprise a more ergonomic form, such that the insulin pump 1
is easier to handle and protrudes as little as possible on the
patient's body. In one embodiment, such as that illustrated in FIG.
2, the underside 3 of the housing 2 may be substantially
rectangular and have rounded corners; however any other operable
configuration may alternatively or additionally be utilized. In one
particular embodiment, except for a narrow edge area, the underside
3 may also be covered with an adhesive coating 4, which may be
provided for securing the insulin pump 1 to the body of a patient,
e.g. in the abdominal area. As also illustrated in FIG. 2, a
circular opening 5 may be formed in the underside 3 of the housing
2, such as centrally on the left-hand side of the housing 2, or
anywhere else about the housing 2. This opening 5 may serve as a
passage for the cannula 11 arranged in the automatic inserter 10 in
the interior of the housing 2. The automatic inserter 10 may be
designed such that it can deploy the cannula 11 from a completely
retracted position in the interior of the housing 2 and through the
opening 5, in an oblique direction with respect to the underside 3,
several millimeters from the opening 5.
Referring now to FIG. 3, a side view of a first lengthwise side 6
of the insulin pump 1 depicts the cannula 11 in the fully deployed
position. The cannula 11 may be made from any soft and
biocompatible material, such as Teflon or the like, and protrude
down to the left in an oblique direction with respect to the
underside 3 of the insulin pump 1. Moreover, in one exemplary
embodiment, in a lower area at the right of the lengthwise side 6
of the housing 2, an infrared interface 50 may be arranged in a
recess of the housing 2 and be used to detect another insulin pump.
To the left alongside it, an optional light-emitting diode 70 may
be located as a status indicator in another recess of the housing
2.
Referring now to FIG. 4, the inner structure of the insulin pump 1
is schematically depicted in a cross section through the housing 2
of the insulin pump 1 along the line A-B from FIG. 3. In one
embodiment, the automatic inserter 10 may be arranged on the
left-hand side, and the inserter 10 communicates with an insulin
reservoir 30 via a tube 33. The insulin reservoir 30 itself may be
arranged in an upper edge area along the upper and second
lengthwise side of the housing 2. Inside the automatic inserter 10,
a tubing system (not shown) may connect the cannula 11 to the tube
33. The insulin 32 present in the insulin reservoir 30 may thereby
be conveyed to the cannula 11 through the tube 33 and the automatic
inserter 10 by means of a delivery device 20 coupled to the insulin
reservoir. In one embodiment, the delivery device 20 may comprise,
for example, a plug (not shown in FIG. 4) which may be moved or
forced into the insulin reservoir 30 by a spindle mechanism, thus
displacing a plug of the insulin reservoir. The insulin 32 located
in the insulin reservoir 30 may thus be displaced by the plug and,
as has been described above, conveyed through the tube 33 into the
cannula 11. In one embodiment, in order to determine the filling
state of the insulin reservoir 30, it may be possible to count the
control impulses sent to a stepping motor of the spindle drive
and/or to provide a motor with an encoder. In another embodiment,
the filling state of the insulin reservoir 30 may be determined by
using a filling state sensor arranged on the insulin reservoir 30.
By way of a control line connecting the filling state sensor to the
control unit 40, the filling state determined in the insulin
reservoir 30 by the filling state sensor can be transmitted to the
control unit 40.
Moreover, in one exemplary embodiment, a sound generator 71, such
as a loudspeaker or buzzer, may be integrated in the area before
the right-hand narrow side of the housing 2 as an additional status
indicator and for alarming purposes. The infrared interface 50,
already described with respect to FIG. 3, may be arranged on the
lower and first lengthwise side 6, in a suitable recess in the
housing 2 to the right of the centre. To its left, the
light-emitting diode 70, arranged on the lower lengthwise side, may
also be arranged in a corresponding further recess in the housing
2. To the left of the centre of the lower and first lengthwise side
6, a radiofrequency interface 60 may also arranged in the interior
of the housing 2. In one embodiment, another communication
interface can be provided instead of the radiofrequency interface
60. For example, an infrared interface can also be used for
transfer of the program as will become appreciated herein.
Referring still to FIGS. 2-4, the first insulin pump 1 and the
second insulin pump 1 may each further comprise a memory 42, a
control unit 40 and a communication interface 60. In one exemplary
embodiment, the control unit 40 with a microprocessor or
microcontroller 41 and the memory unit 42 may be arranged in the
central area in the interior of the insulin pump 1. For example,
the control unit 40 may be connected to the inserter via a first
control line 110, such that the insertion and optionally also the
retraction of the cannula 11 can be controlled by the control unit
40. A second control line 120 between the control unit 40 and the
delivery device 20 may permit the transfer of control impulses from
the control unit 40 to the delivery device 20. In such an
embodiment, the sound generator 71 discussed above may be connected
by a third control line 171 to the control unit 40 and can thus be
activated by the latter. Furthermore, the light-emitting diode 70
may likewise be connected by a fourth control line 170 to the
control unit 40 and can be switched on or off by the latter. The
fifth control line 150 between the infrared interface 50 and the
control unit 40 may permit the activation and deactivation of the
infrared interface 50 and also the data transfer between infrared
interface 50 and control unit 40. Finally, the radiofrequency
interface 60 may be connected to the control unit 40 by the sixth
control line 160. Between control unit 40 and radiofrequency
interface 60, data may be transferred and the radiofrequency
interface 60 can be activated or deactivated. In one embodiment,
above the sectional plane illustrated in FIG. 4, a battery 80 may
be present for the insulin pump 1 (indicated by the broken line).
The cabling of the battery 80 may be configured in a manner
known.
The memory unit 42 may be provided both for storage of a infusion
program and also for holding a protocol file (such as selected
operating parameters of the insulin pump) or log file of the
insulin pump. As used herein, the term `infusion program` is used
in the sense of data and parameters necessary for the insulin pump
to operate as intended. The infusion program may comprise a
patient-specific basal delivery schedule as well as the current
time of day and/or the current date. For example, an operation mode
in which the first insulin pump 1 or the second insulin pump 1
performs delivery according the infusion program may be referred to
as the `delivery mode`.
In one particular embodiment, the memory 42 may specifically be
configured to store the infusion program, the control unit 40 may
be configured to control the operation of either the first insulin
pump 1 or the second insulin pump 1. The communication interface 60
may be configured for data exchange with the other of the first
insulin pump 1 and the second insulin pump 1. In one embodiment,
the control unit 40 of the first insulin pump 1 may be configured
to autonomously perform the steps of activating a search for the
presence of the second insulin pump 1, and, upon detection of the
presence of the second insulin pump 1 transmitting, via the
communication interface 60 of the first insulin pump 1, the
infusion program stored in the memory 42 of the first insulin pump
1 to the second insulin pump 1.
Furthermore, the control unit 40 of the second insulin pump 1 may
be configured to perform the steps of searching for the presence of
the first insulin pump 1, and, upon detection of the presence of
the first insulin pump 1 performing the steps of receiving, via the
communication interface 60 of the second insulin pump 1, an
infusion program from the first insulin pump 1, and storing the
infusion program in the memory 42 of the second insulin pump 1.
In one embodiment of continuing therapy via a second insulin pump
1, the infusion program may be the basis for an appropriate insulin
infusion according to the patient's individual need. Thus, in
contrast to the basal administration, the additional insulin boli
may also be administered whenever required by alternative means,
such as an insulin pen or a syringe. Therefore, an insulin infusion
system according to one embodiment may allow the patient to
continue his or her therapy even if no remote controller is present
and/or if the insulin pumps have no user interface for initiating
or modifying the drug administration. In one embodiment of the
insulin infusion system, the pump replacement may allow for a
simple use thereof via the detection of the presence of the second
insulin pump and the subsequent transfer of the infusion program
being carried out autonomously without the need for user
interactions.
In one exemplary embodiment, the first insulin pump 1 and the
second insulin pump 1 of the system may be designed or configured
such that the first insulin pump 1 only has the capability of
transmitting the infusion program to the second insulin pump 1 and
the second insulin pump 1 only has the capability of receiving an
infusion program from the first insulin pump 1. Alternatively,
either of the two insulin pumps 1 may both transmit and receive an
infusion program. In particular embodiments, however, the first
insulin pump 1 and the second insulin pump 1 may comprise identical
insulin pumps, each being generally capable of acting as the first
insulin pump 1 or as the second insulin pump 1. As discussed above,
both insulin pumps 1 may comprise disposable insulin pumps which
may be provided in a kit of, for example, ten individual pumps.
Alternatively, the first insulin pump 1 may, for example, be the
generally used insulin pump while the second insulin pump 1 may be
an additional backup pump.
In yet another embodiment, the insulin pump 1 may generally
comprise a communication interface for data exchange with a
replacement pump, a memory which is configured to store an infusion
program, and a control unit which is configured to control
operation of the insulin pump 1. The control unit of the insulin
pump 1 may be configured to autonomously perform the steps of
activating a search for the presence of the replacement pump, and
transmitting, upon detecting the presence of the replacement pump,
via the communication interface the infusion program stored in the
memory to the replacement pump.
In one embodiment, the insulin pump 1 may comprise an insulin pump
1 of an insulin infusion system and may be used in an insulin pump
replacement method as will become appreciated herein. Therefore,
the disclosed embodiments of the insulin pump 1 and its operation
also define corresponding embodiments of the insulin pumps 1 in an
insulin infusion system and of the method for replacing a first
insulin pump 1 by a second insulin pump 1. For example, the insulin
pump 1 may be configured to perform the steps of searching for the
presence of a source pump, and, when the presence of a source pump
is detected, performing the steps of receiving, via the
communication interface, an infusion program from the source pump,
and storing the infusion program in the memory. An insulin pump of
this type of embodiment may be capable of alternatively serving as
both the first insulin pump 1 or the second insulin pump 1 in an
insulin infusion system and a replacement method as described
herein.
In one embodiment, the communication interface 60 via which an
infusion program may be transmitted from a source pump to a
replacement pump may comprise a wireless bidirectional
communication interface 60 which can allow simple data exchange.
The communication interface 60 may, for example, comprise a radio
frequency interface according to a communication standards known in
the art, such as the BLUETOOTH standard, or according to a
proprietary standard. Alternatively, the wireless bidirectional
communication interface 60 may comprise an infrared interface. In
further alternative embodiments, the communication interface 60 may
comprise a wired interface.
When a remote controller is present, data may be exchanged with the
remote controller via the same communication interface 60 of the
insulin pump 1. Alternatively, the insulin pump 1 may comprise a
separate communication interface 60 for communicating with a remote
controller. Thus, in one embodiment, the insulin pump 1 may be
configured to receive its infusion program from a remote controller
in the alternative to receiving it from a source pump 1.
As discussed above, an insulin pump 1 may act as source pump. In
such embodiments, the control unit 40 may be configured to monitor,
during operation of the insulin pump 1 according the infusion
program, a status of the insulin pump 1 and to activate the search
for the presence of a replacement pump 1 when a predetermined
status is assumed by the insulin pump 1.
Furthermore, in one particular embodiment, searching for a
replacement pump 1 may only occur if a predetermined status is
assumed. Such an embodiment may limit energy consumption as well as
avoid handling errors since it prevents an unintended program
transfer. The status of the insulin pump 1 may also be checked in a
test mode which is periodically activated by a timer of the control
unit 40. Alternatively or additionally, the search for a
replacement pump 1 may be activated by an interrupt signal which is
generated when the predetermined status is assumed. In such an
embodiment, a dedicated test mode may not be required.
In another embodiment, the status of the insulin pump 1 which may
be monitored during operation may comprise a filling state of the
insulin reservoir. In such an embodiment, a search for another pump
to act as replacement pump may thereby be activated if the filing
volume of the insulin reservoir falls below a predefined value of,
e.g. 10%, of the maximum filling volume. In another embodiment, the
status may further comprise an error status, such that the
occurrence of an error condition, i.e. an occluded infusion cannula
or a device error, may be periodically monitored and a search for
another insulin pump may be activated upon the occurrence of an
error condition.
In one exemplary embodiment, the status may further comprise the
status of a battery 80 of the insulin pump 1. Such an embodiment
may be utilized, for example, when the battery 80 is integral with
the pump 1 and cannot be replaced. While the battery 80 capacity of
these types of devices may include a safety factor to ensure that
the battery 80 is not exhausted prior to the reservoir being empty,
this situation may nonetheless occur if the battery is, due to
improper assembly, partly discharged during assembly of the
infusion pump, or due to a defective of the battery 80 itself, or
the like. Therefore, the battery voltage may be monitored by a
voltage monitoring unit in an analogue way to the filling volume of
the insulin reservoir. Additionally or alternatively to the
voltage, the energy effectively taken from the batter may be
monitored by a gauging unit known in the art.
In some embodiments, the source pump 1 may transmit the status of
the source pump to the replacement pump 1 along with the infusion
program. For example, it may transmit an error code of an error
which can result in the source pump activating the search for a
replacement pump 1.
In another Embodiment, the insulin pump 1 may be designed such that
insulin delivery may be continued during the search for a
replacement pump 1. For example, if the search is activated because
of the filling state of the insulin reservoir 30 falling below a
predefined value as described above, the delivery may be continued
until the program is transferred to a replacement pump 1 such that
the insulin delivery is not interrupted longer than required.
The control unit 40 may also be alternatively or additionally
configured to control the insulin pump 1 to terminate operation
after successful transmission of the infusion program to the
replacement pump 1. Terminating the operation may, for example,
comprise stopping the insulin delivery, followed by switching off
the pump or changing it a safe state. In one embodiment, it may
further comprise an automated rejection of the infusion cannula by
an inserter of the insulin pump.
As also discussed above, an insulin pump 1 may also act as a
replacement pump 1. For example, in embodiments of the insulin pump
1 which allow the insulin pump 1 to act as replacement pump 1, the
control unit 40 may be configured to control the insulin pump 1,
after successfully having received an infusion program from the
source pump 1, to automatically start insulin delivery. Starting
the insulin delivery may additionally comprise preparative steps,
in particular priming the infusion cannula with insulin and/or
inserting the infusion cannula 11 into the patient's subcutaneous
tissue by an automatic inserter of the insulin pump 1. Automatic
insertion of the infusion cannula 11 may be employed, for example,
if the insulin pump 1 is a patch pump which is secured to the
patient's skin via an adhesive layer.
In another embodiment, an insulin pump 1 may allow for a simple
replacement or exchange, and, thus, continuation of the therapy,
without requiring the presence of a remote controller and without
requiring the presence of operation elements, such as buttons or a
display, on the pump. Thus, since all required steps are performed
automatically under control of the two pumps, the patient may
simply secure the newly programmed replacement pump 1 to his or her
body after the transfer of the infusion program is complete.
In some embodiments where the infusion cannula 11 of the
replacement pump 1 is automatically inserted into the skin, the
control unit 40 of the replacement pump 1 may be configured to
wait, after the replacement pump 1 has successfully received the
infusion program, for a defined period of time before actuating the
inserter. This defined period of time between the transfer of the
program and the insertion of the cannula 11 may provide the patient
sufficient time to secure the insulin pump to the body. For
example, in one embodiment, a time period of 10-15 minutes may be
provided. In another embodiment, a time period of longer than 15
minutes for insertion of the cannula may be provided. In yet
another embodiment, shorter waiting time of less than 10 minutes
may be provided.
As long as the insulin pump 1 which is acting as replacement pump 1
is not in use and has not received an infusion program from a
remote controller or a source pump 1, it may be sustained in a
low-energy mode. For example, as described above, disposable pumps
may be provided with a readily built-in battery. Since the size of
such a battery is limited by the overall device dimensions and the
pump may be stored for several weeks or months prior to its use,
providing the insulin pump low-energy mode may provide for minimum
energy consumption and elongate the lifespan of the device.
In one embodiment, as the insulin pump 1 is in the low energy mode,
the insulin pump 1 may be periodically switched into a search mode
to detect the presence of a source pump 1 or remote controller. The
time interval may, for example, be 1 second, 1 minute or 3 minutes.
Similarly, an additional device for detecting another insulin pump
may be activated periodically in a search mode. Setting the time
interval may thereby require a compromise between a short delay for
detecting the presence of a source pump on the one hand and low
energy consumption on the other hand. Thus, the time delay may be
adjusted based on the particular application of the insulin
pump.
As discussed above, communication between a source pump 1 and a
second pump 1 may allow for the transfer of the infusion program.
In one embodiment both an insulin pump 1 acting as source pump 1 as
well as an insulin pump 1 acting as replacement pump 1 may operate
in a search mode. As used herein, the term `search mode` is used
for a mode where the pump searches for the presence of an other
insulin pump 1, but a communication line has not yet been
established. The search mode may be either active or passive. If
the search mode is active, the insulin pump 1 may emit signals,
such as infrared or radiofrequency signals, to be received and
responded to by the other insulin pump 1. If the search mode is
passive, the insulin pump 1 may wait for the reception of signals
emitted by the other insulin pump 1 and responds to such received
signals. In one embodiment, the search mode is active if the
insulin pump 1 serves as a source pump 1. In another embodiment,
the search mode is passive if the insulin pump 1 serves as a
replacement pump 1. In yet another embodiment, other search mode
assignments to the various insulin pumps may additionally or
alternatively be made.
In some embodiments, the communication interface 60 which is used
for transmitting the infusion program of the source pump 1 to the
replacement pump 1 may also be used for detecting the presence of
the other of the source pump 1 and the replacement pump 1,
respectively. Alternatively, the insulin pump 1 may also have an
additional device for detecting another insulin pump. In such an
embodiment, the detection of another insulin pump 1 may take place
independently of the communication interface 60 which is used for
the data exchange. While requiring additional hardware, this may
allow for the communication interface 60 only being activated after
the detection of the other insulin pump 1 thereby providing
additional energy consumption and safety.
In one embodiment, switches or sensors may be utilized to detect
magnetic and/or electric fields. However, purely mechanical
switches could additionally or attentively be provided, which may,
for example, be activated by a coupling member, such as a notch, of
the other insulin pump 1. In one particular embodiment, the device
for detecting another insulin pump 1 may comprise a reed relay or a
Hall sensor. For example, in one particular embodiment, a reed
relay may be used to detect magnetic fields, that are generated,
for example, by a permanent magnet or an electro magnet in the
other insulin pump. This may provide a particularly
energy-efficient embodiment as the reed relay itself does not
require current, and the energy for changing the switch state may
be introduced into the insulin pump from outside. In another
particular embodiment, a Hall sensor may be used to detect the
other insulin pump. In such an embodiment, when the Hall sensor has
a current passed through it and is brought into a magnetic field
running perpendicular to it, it may deliver an output voltage. A
switch function may thus be obtained in combination with a
transistor and/or further semi-conductor components known in the
art. In this way, as in the case of the reed relay, the magnetic
fields of permanent magnets arranged in the other insulin pump can
be detected. The Hall sensor may allow for no mechanically movable
parts that could be damaged such as, for example, if the insulin
pump were accidentally dropped.
For embodiments comprising a magnetic-field sensitive switch or
sensor, the device for detecting another insulin pump may further
comprises a magnet, such as a permanent or an electro magnet for
generating a magnetic field. The magnet may thereby activate the
magnetic field-sensitive switch or sensor in the other insulin
pump. By approaching the insulin pumps 1, the magnetic field
generated by the magnet in either of the insulin pumps may activate
the magnetic-field sensitive switch or sensor of the other the
other insulin pump. In one embodiment, the magnet and the
magnetic-field sensitive switch or sensor may be arranged in a
substantially shielded position from each other or at sufficiently
spaced positions from the insulin pump 1, such that the switch or
sensor is not operated by the magnet of the same pump. The magnet
and the magnetic-field sensitive switch or sensor may be designed
for an activation distance of some centimeters or for activation
only if the insulin pumps 1 touch each other. In one embodiment, a
well defined orientation of the insulin pumps 1 with respect to
each other may further be required for the magnetic-field sensitive
switch or sensor to be activated.
In some embodiments, it may be sufficient if the magnetic-field
sensitive switch or sensor of one of the pumps, for example the
replacement pump, is activated by a magnetic field emitted by the
other insulin pump 1. In some of those embodiments, the insulin
pump may comprise, for example, an electro magnet which is powered
only in the search mode. Alternatively, the insulin pump 1 may be
designed such that a program transfer may only be performed if the
magnetic-field sensitive switch or sensor of both of the two pumps
is activated by the other of the two pumps.
In another embodiment, the device for detecting the other insulin
pump 1 may be designed as an infrared interface. In addition, coded
signals may also be transmitted with an infrared interface such
that, before the actual data exchange via the bidirectional
communication interface 60, it is possible to verify whether both
communicating devices are compatible insulin pumps 1.
For embodiments comprising a switch which has to be activated
before an infusion program can be transferred to it, a remote
controller may be configured to activate the switch in the same or
similar way as a source pump.
In embodiments comprising a switching element, such as a mechanical
switch or a reed relay as device to detect the presence of another
insulin pump 1, the insulin pump 1 may be switched off in the
low-energy mode. Only activating the switch may result in the
controller of the pump to be powered. Once the insulin pump is in
operation, the components of the insulin pump 1 may be connected
with the battery by a further relay, semiconductor switch, or the
like, such that activation of the switch by en external energy is
not further required. For this type of embodiment, the insulin pump
may not consume any energy in the low-energy mode since it does not
need to periodically activate a communication interface or a device
for detecting another insulin pump since the energy for switching
the switch and, thus, changing the operation mode of the insulin
pump 1 is introduced into the insulin pump from outside, that is,
from the other insulin pump 1.
In one particular embodiment in which the insulin pump comprises an
electro magnet for activating a magnetic-field sensitive switch of
another insulin pump 1, it may be designed such the electro magnet
of the source pump is powered in the search mode, while the electro
magnet of the replacement pump is not powered in the low-energy
mode and search mode. Such an embodiment may not require the
replacement pump to emit energy while in the low energy mode and
thus require only minimum energy consumption of the unused
replacement pump prior to its application. After the magnetic-field
sensitive switch or sensor of the receiving pump has been activated
by the source pump, it may optionally power its electro magnet to
activate the magnetic-field sensor or switch of the source pump for
acknowledging purposes.
As stated above, the insulin reservoir of the pump is typically in
an initial empty state and is filled by the patient prior to use.
In some embodiments, the insulin pump may be designed such that
filling of the insulin reservoir is automatically detected. Upon
detecting of the insulin reservoir being filled, the insulin pump
may switch to the search mode. If the pump is of the syringe-driver
type, a plug of the insulin reservoir may be in an initial most
proximal position corresponding to an empty drug reservoir and
displaced into a distal position if fluid is forced into the
insulin reservoir, e.g., via a syringe. In such an embodiment, the
pump may be designed such that this displacement of the plug
operates an electrical contact which triggers the pump to switch to
the search mode. Likewise, before the contact is operated, the
insulin pump may be switched off.
In some embodiments, the insulin pump 1 may comprise indicators
such as light emitting diodes, a buzzer or loudspeaker, a pager
vibrator, or the like. Those indicators may be used to indicate one
or multiple of a number of situations. In particular, the
indicators may indicate at least one of the search for the
replacement pump, the successful detection of the replacement pump,
the successful transmission of the program to the replacement pump,
or the unsuccessful transmission of the program to the replacement
pump.
In embodiments of the insulin pump 1 which may act as replacement
pump, an indication unit may be configured to indicate at least one
of the search for the source pump being active, the establishment
of communication with the source pump, the successful reception of
the infusion program from the replacement pump, the unsuccessful
reception of the infusion program from the replacement pump, or the
start of insulin delivery.
While reference has been made herein to particular insulin delivery
systems and insulin pumps, the utilization of such systems and
pumps may provide for continuous therapy for a patient. For
example, according in one embodiment, the method of replacing a
first insulin pump with a second insulin pump may comprise the
steps of operating the first insulin pump according to an infusion
program stored in a memory 42 of the first insulin pump, and
autonomously performing the steps of activating a search for the
presence of the second insulin pump, and, upon detection of the
presence of the second insulin pump transmitting, via communication
interfaces 60 of the first insulin pump and the second insulin
pump, the infusion program from the first insulin pump to the
second insulin pump.
In another embodiment, the method may further comprise the step of
monitoring, during operation of the first insulin pump according
the infusion program, a status of the first insulin pump and
activating the search for the presence of the second insulin pump
when a predetermined status is assumed by the first insulin pump.
For such an embodiment, the search for the presence of the second
insulin pump is carried out if the status of the first insulin pump
indicates that it should be replaced by the second insulin
pump.
Referring now to FIG. 1 (i.e., FIGS. 1a, 1b, 1c and 1d), a
schematic illustration of transitioning between a first insulin
pump 505 and a second insulin pump 505' is shown. Specifically,
FIG. 1a depicts a first insulin pump 505 in accordance with one
exemplary embodiment which may be attached to the skin 502 of a
patient and is presently in the delivery mode. The first insulin
pump 505 may have received its infusion program from a remote
controller 510 or from a previously used insulin pump. The
additional infusion of insulin boli, as well as further programming
and control capabilities for the first insulin pump 505, may be
available via the remote controller 510. FIG. 1b further depicts a
second insulin pump 505' which is of the same type as the first
insulin pump 505. The second insulin pump 505' may be provided, for
example, in a sterile box 515 and in a low-energy mode or sleeping
mode.
FIG. 1b depicts a later situation where a status of the first
insulin pump 505 is such that it may be replaced due to the filling
state of its insulin reservoir, the status of the battery and/or
the occurrence of an error condition. In such a condition, the
first insulin pump 505 may give an indication to the patient via an
acoustical and/or optical indicator and activate the search for a
second insulin pump. Upon the indication, the patient may remove
the second insulin pump 505' from its sterile box 515 and
transition it towards the first insulin pump 505. Prior to
performing this step, the patient may also fill the insulin
reservoir of the replacement pump 505' if it was initially empty.
In the following, the first insulin pump 505 acts as source pump
while the second insulin pump 505' acts as replacement pump. The
presence of the replacement pump 505' may be detected by the source
pump 500 and communication may be established as indicated by the
arrows 520.
After establishing the communication, the source pump 505 may
transfer the infusion program to the replacement pump 505' as
indicated in FIG. 1c by arrow 525. After successful transmission of
the infusion program, the source pump 505 may terminate its
operation.
The final steps of the exemplary replacement procedure are shown in
FIG. 1d. Specifically, the patient may remove the source pump 505
from its skin 502 and discard it, as indicated by arrow 530. The
patient may then attach the replacement pump 505' to his or her
skin 502. After a delay of some minutes, the replacement pump 505'
may carry out preparative steps, such as, for example, priming its
infusion cannula with insulin and inserting the infusion cannula
into the patient's subcutaneous tissue and subsequently start
insulin infusion. If the insulin pumps do not comprise an infusion
cannula which is automated inserted into the patient's tissue, this
step may be carried out manually by the patient.
Referring now to FIGS. 2-5, an exemplary method is illustrated in
FIG. 5 in which the insulin pump 1 functions as the source pump.
Specifically, the insulin pump 1 may initially be in the delivery
mode 200. The insulin pump 1 may then deliver insulin 32 via the
delivery device 20 and supply the patient with the required doses
of insulin 32 in accordance with a basal delivery schedule which is
stored as infusion program in the memory unit 42. On the basis of
the number of control impulses already sent to the delivery device
20, the control unit 40 additionally determines the filling state
of the insulin 32 in the insulin reservoir 30. In one embodiment,
the light-emitting diode 70 (when present) may be additionally used
to signal the delivery mode.
In the subsequent test mode 201, the determined filling state of
the insulin reservoir may be compared to a minimum value stored in
the memory unit 42. If the filling state is greater than or equal
to the minimum value, the operation may be changed back to the
delivery mode 200 and the filling state may be determined again
after a period of time and/or after a following insulin delivery.
However, if the control unit 40 determines in the test mode 201
that the filling state is less than the minimum value stored in the
memory unit 42, the first interface activation 202 may take place
in which the infrared interface 50 is switched on. In the same way,
the occurrence of an error condition, such as a device error or an
occluded cannula, may be monitored in the test mode 201.
Optionally, the state of the battery 80 may also be determined and
compared to a minimum value in an analogue way to the insulin
reservoir.
The control unit 40 may then change to the search mode 203, in
which the insulin pump 1 searches for an infrared signal from a
second and unused replacement pump. If no such signal is detected,
the control unit 40 may change to the interface deactivation mode
204. In the interface deactivation mode 204, the infrared interface
50 may be first switched off and then after a period of 2 minutes,
for example, may be allowed to elapse before the control unit 40
performs the first interface activation 202 again.
As soon as an infrared signal of a replacement pump is detected
during the search mode 203, the insulin pump 1 may test whether the
infrared signal has a known and valid code. If no code is
recognized, the insulin pump 1 may change back to the interface
deactivation mode 204. However, if the code of the infrared signal
is recognized by the insulin pump 1, the control unit 40 may change
to the connection mode 205. An acknowledgement signal may be sent
to the replacement pump via the infrared interface 50, and the
radiofrequency interface 60 may then switched on. A connection to
the replacement pump detected by the infrared interface 50 may then
be set up via the radiofrequency interface 60. Among other things,
the data transfer rates may be established on the basis of the
signal quality.
In the subsequent transmit mode 206, the infusion program stored in
the memory 42 of the insulin pump 1 may be transferred to the
replacement pump via the radiofrequency interface 60. After the
data transfer has taken place, the insulin pump 1 may change to the
switch-off mode 207 in which operation of the insulin pump 1 is
terminated. In the switch-off mode 207, a standby time, for example
of 2 minutes, may be allowed to elapse. The control unit 40 may
then deactivate the delivery device 20 and thus stop the delivery
of insulin 32. Thereafter, the control unit 40 may optionally cause
the inserter 10 to retract the cannula 11. The control unit 40 may
then emit an acoustic signal via the sound generator 71 to indicate
termination of the operation and switch off all the other
components of the insulin pump 1. The insulin pump 1 can then be
removed by the patient from his or her body and, for example,
replaced by the replacement pump.
The insulin pump 1 may thus supply the patient with insulin
throughout all the method steps or modes 200-206 illustrated in
FIG. 2, except in the switch-off mode 207. In case of an error, the
insulin delivery may be terminated and the insulin pump may emit an
alert signal via the sound generator 71 and/or the light-emitting
diode 70 throughout the modes 200-206. Alternatively, insulin
supply may be stopped between establishing the connection in step
205 and transmitting the program in step 206.
Referring now to FIGS. 2-4 and 6, an exemplary method is
illustrated in FIG. 6 in which the insulin pump 1 functions as the
replacement pump. Specifically, the method illustrated in FIG. 6
shows the mode of operation of the insulin pump 1 (as a replacement
pump) provided in the unused state and upon first activation. After
production, the insulin pump 1 may be in the low-energy mode 400
and not yet possess a patient-specific program in its storage. In a
first step 401, a coded infrared signal may be emitted via the
infrared interface 50 in the low-energy mode 400. In the second
step 402 of the low-energy mode 400, the infrared interface 50 may
search for an acknowledgement signal from another insulin pump
(which acts as source pump and accordingly has a patient-specific
program). If no acknowledgement signal is detected, the first step
401 of the low-energy mode 400 may be performed again. The steps
401 and 402, form in combination, a search mode of the insulin pump
1. The steps may optionally be performed only after filling of the
insulin reservoir 30 of the insulin pump 1 by the patient has been
detected. In such an embodiment, the low-energy mode may thereby be
equivalent with the search mode. In an other embodiment, the
acknowledgement signal received in the second step 402 of the
low-energy mode 400 may originate from a remote controller and,
accordingly, the program may transfer from the operating appliance
to the insulin pump in the receive mode. This may comprise the
normal case where an operational remote controller is present.
As soon as an acknowledgement signal is detected in the second step
402 of the low-energy mode 400, the control unit 40 may activate
the radiofrequency interface 60 in the switch-on step 403. A
connection may then be set up with the other insulin pump detected
by the infrared interface 50 and, among other things, the data
transfer rate may be established on the basis of the signal
quality.
In the subsequent receive mode 404, the program of the other
insulin pump may be transferred to the insulin pump 1 via the
radiofrequency interface 60 and stored in the memory unit 42. The
program may include in particular the time and date as well as the
basal delivery schedule.
Thereafter, the control unit 40 may change to standby mode 405,
during which the insulin pump 1 shows no activity for a period of,
for example, 15 minutes. The standby mode 405 may give a patient
sufficient time to apply the insulin pump 1 to the desired location
on the body. After the 15 minutes have passed, the insulin pump may
change automatically to the use mode 406, in which the control unit
40 causes the inserter 10 to deploy the cannula 11 and thus insert
it into the patient's body. Before changing to the standby mode
405, the cannula 11 may optionally be automatically primed in order
to displace the air in the cannula 11 by insulin.
The control unit 40 may then change to start-up mode 407. The
delivery device 20 may thereby be activated by the control unit 40
and deliver insulin 32 from the insulin reservoir 30 into the
cannula 11 according to the program stored in the memory unit 42.
The control unit 40 may also emit an acoustic signal via the sound
generator 71 and optionally indicate beginning of the delivery via
the light-emitting diode 70. The control unit may then change to
the delivery mode 200 described in FIG. 5.
With respect to FIG. 5, the insulin pump, may, in the search mode
203, emit an infrared signal to be detected by a replacement pump
rather than searching for an infrared signal emitted by a
replacement pump, followed by searching for the reception of an
acknowledgement signal to be sent by a replacement pump.
In an analogue way, with respect to FIG. 6, the insulin pump 1 may,
in the mode 401, detect if an infrared signal is received from a
source pump rather than emitting a signal. In such an embodiment,
the step 402 may be omitted. An acknowledgement signal is, in this
case, emitted by the insulin pump 1 in the switch-on-step 403.
As discussed above, other devices for providing signals and
information to the user can be used instead of or in addition to
the light-emitting diode 70 or the sound generator 71. For example,
in one embodiment, the sound generator 71 can be replaced by a
tactile element, such as a mechanical vibrator. In another
embodiment, a screen may be provided for displaying symbols or
texts which, for example, provide information on the operating
state of the insulin pump. Furthermore, in another embodiment, the
infrared interface 50 for detection of a replacement pump may be
omitted and a reed relay or a Hall sensor may be provided as
discussed above. In such an embodiment, a permanent magnet may also
be disposed in the interior of the housing 2, such that the insulin
pump 1 can also be detected by a replacement pump. The reed relay
or Hall sensor may thus be activated only when a filling state of
an insulin reservoir of the source pump falls below a predefined
minimum value, in particular 10%, and/or on the occurrence of an
error condition or another predetermined status of the source pump.
Such an embodiment may allow for the reduction in the risk of
inadvertent actuation through magnetic interference sources.
It is noted that the terms "substantially" and "about" may be
utilized herein to represent the inherent degree of uncertainty
that may be attributed to any quantitative comparison, value,
measurement, or other representation. These terms are also utilized
herein to represent the degree by which a quantitative
representation may vary from a stated reference without resulting
in a change in the basic function of the subject matter at
issue.
While particular embodiments have been illustrated and described
herein, it should be understood that various other changes and
modifications may be made without departing from the spirit and
scope of the claimed subject matter. Moreover, although various
aspects of the claimed subject matter have been described herein,
such aspects need not be utilized in combination. It is therefore
intended that the appended claims cover all such changes and
modifications that are within the scope of the claimed subject
matter.
* * * * *